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Max was known by his nickname, “Little Dude,” but there was nothing “little” about Max and how he touched so many people in his short life.
When he was five, he started Kindergarten … and was so excited about going to the same school his big sister attended. Max, was a vibrant little boy who loved Star Wars, Legos and sushi. Two days before Halloween, at the age of five, he was diagnosed with one of the rarest, deadliest, and most aggressive forms of cancer- Diffuse Intrinsic Pontine Glioma (DIPG). Less than 10% of the 100-150 kids diagnosed each year live beyond 18 months from diagnosis. In Max’s case, he survived only nine more months, until the fourth of July.
Out of love for Max and the determination to help other families facing this cancer diagnosis, Max’s family and friends established The Max Lacewell Foundation to bring awareness and find a cure for brain stem glioma tumors. Over the last three years, our 100% volunteer run organization has raised over $400,000 for Lurie Children’s Hospital of Chicago with the hopes of ultimately establishing a research scholar dedicated to DIPG.
Max lives on in the hearts of the many people he connected with … and we are determined to do what we can to help find the cure for DIPG so other “little dudes and dudettes” can have more powerful weapons against this cancer.
This site provides connections with:
Max Lacewell Foundation – a place where you can learn more about research into DIPG and donate to finding a cure.
Celebrating Max – gives you a way to connect with Max’s family and a place to remember this special “little dude.”
P.O. Box 9715, Naperville, IL 60564
The Max Lacewell Foundation is an IRS approved non-profit. FEIN 27-2288263.